Anti-fibrotic effect of ketoprofen-grafted alginate ... - ACS Publications

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Anti-fibrotic effect of ketoprofen-grafted alginate microcapsules in the transplantation of insulin producing cells François Noverraz, Elisa Montanari, Joël Pimenta, Luca Szabo, Daniel Ortiz, Carmen Gonelle-Gispert, Léo Bühler, and Sandrine Gerber-Lemaire Bioconjugate Chem., Just Accepted Manuscript • DOI: 10.1021/acs.bioconjchem.8b00190 • Publication Date (Web): 22 May 2018 Downloaded from http://pubs.acs.org on May 29, 2018

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Bioconjugate Chemistry

Anti-fibrotic effect of ketoprofen-grafted alginate microcapsules in the transplantation of insulin producing cells

François Noverraz,1‡ Elisa Montanari,2‡ Joël Pimenta,2 Luca Szabó,1 Daniel Ortiz,3 Carmen Gonelle-Gispert,2 Léo H. Bühler,2 Sandrine Gerber-Lemaire1*

1

Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne,

Group for Functionalized Biomaterials, EPFL SB ISIC SCI-SB-SG, Station 6, CH-1015 Lausanne, Switzerland 2

University Hospital of Geneva, Surgical Research Unit, CMU-1, CH-1211 Geneva,

Switzerland 3

Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne,

SSMI, Batochime, CH-1015 Lausanne, Switzerland ‡

These authors contributed equally to the work

ABSTRACT The controlled release of small molecular modulators of the immune response from hydrogel microspheres (MS) used for cell immobilization is an attractive approach to reduce pericapsular fibrotic overgrowth (PFO) after transplantation. Ketoprofen is a well-known nonsteroidal anti-inflammatory drug involved in the early stage inflammation cascade. PEGylated derivatives of ketoprofen, presenting either ester or amide linkage to the drug, were synthesized and conjugated to the hydroxyl groups of sodium alginate (Na-alg). Functionalized cell-free and MIN6 cells containing MS were produced from the resulting modified alginates. In vitro quantification of ketoprofen release indicated regular and sustained drug delivery over 14 days, resulting from the hydrolytic cleavage of the ester bond. 1 ACS Paragon Plus Environment

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The release kinetics was enhanced over the initial 7 days by the presence of MIN6 cells, probably as a result of cell esterase activity. In the presence of amide bond, traces of ketoprofen were released over 14 days due to a much slower hydrolysis kinetics. Cell-free and MIN6 cells containing MS were transplanted in immune-competent mice, either in the peritoneal cavity or under the kidney capsule, with a follow-up period of 30 days. Comparison with non-modified Ca-alg MS transplanted in the same conditions demonstrated a clear reduction in the severity of PFO for MS functionalized with ketoprofen. Quantification of collagen deposition on MIN6 cells containing MS transplanted under the kidney capsule revealed the significant effect of ketoprofen release to decrease fibrotic tissue formation. The impact was more pronounced when the drug was covalently conjugated by an ester linkage, allowing higher concentration of the anti-inflammatory compound to be delivered at the transplantation site. The functionality of microencapsulated MIN6 cells 30 days after transplantation was confirmed by detection of insulin positive cell content.

KEYWORDS.

Alginate

derivatives;

Antifibrotic

effect;

Biocompatibility;

Cell

microencapsulation; Controlled release; Covalent grafting; Fibrosis; Functionalized hydrogels; Ketoprofen

INTRODUCTION The low availability of human donor material to replace dysfunctional cells, damaged tissues and end-stage diseased organs have prompted the search for alternative transplantation strategies. Initiated by Chang1 in 1964 who proposed the concept of "artificial cells", the microencapsulation of cells and tissue appears as a promising strategy for the development of allo- or xenotransplantation therapies.2-4 This technology has been widely studied for the immuno-isolated transplantation of endocrine cells, in particular toward the treatment of

2 ACS Paragon Plus Environment

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hepatic diseases5 and type I diabetes.6 The main function of the encapsulation materials is to prevent the passage of immune cells and antibodies, while enabling the bidirectional diffusion of molecules essential for cell survival and metabolism such as nutrients and oxygen, and the release of metabolic products.7,8 In addition to isolation from the host immune response, the semi-permeable immobilization matrix offers supportive structure for cells and protection against mechanical stress and deteriorating environmental effects. These combined properties have the potential to avoid or strongly reduce the use of chronic immunosuppression and to overcome the critical human donor shortage by the transplantation of encapsulated nonhuman cells.9 Due to its advantageous gelling properties in contact with divalent cations such as Ba2+ and Ca2+,10 sodium alginate (Na-alg) is by far the most widely employed polymer for cell microencapsulation. Despite the high cell compatibility of hydrogels prepared from Naalg and derivatives,11,12 the clinical applications of alginate-based hydrogels for cell transplantation are severely hindered by the lack of in vivo mechanical durability, defects in permselectivity and low host biocompatibility resulting in pericapsular fibrosis, cell necrosis and loss of graft functionality.13-17 Several strategies have been highlighted to increase the stability of alginate microspheres (MS). The coating with polycations such as poly(L-lysine) and poly(L-ornithine) reinforced the mechanical properties of alg-based hydrogels but resulted in the adverse activation of inflammatory cytokines and growth factor in vivo.18,19 The performance of alg MS, in particular their suitability for cell microencapsulation as well as their elasticity and selective permeability, could be largely improved by combination with poly(ethylene glycol) (PEG) chains equipped with complementary end reactive functionalities allowing the electrostatic network formed with divalent cations to be reinforced by covalent crosslinking from PEG derivatives.20-23 Various approaches were reported to try to reduce pericapsular fibrotic overgrowth. Vaithilingam et al. showed that the co-encapsulation of hepato cellular carcinoma cells HuH7 with mesenchymal stem cells (MSCs), which are



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known to secrete several small molecular modulators of the immune response after activation, produces a dose-dependent effect on reducing pericapsular fibrosis in a stringent xenotransplantation setting.24 A recent study by the same group demonstrated that murine MSCs co-encapsulated with islets reduced fibrotic overgrowth and improved allograft survival in diabetic mice.25 The beneficial effect of microencapsulated human MSCs on liver fibrosis was also observed in bile duct ligation-induced liver fibrosis in mice.26 Different studies indicated that the co-encapsulation of pancreatic islets with anti-inflammatory and immunosuppressive drugs, enhanced the function of encapsulated cells and reduced fibrosis.27-29 In particular, the co-encapsulation of curcumin with rat islets in alg MS improved glycemic control in diabetic mice and mitigated the formation of fibrotic tissue.28 Finally, high purity of the encapsulating alg material30 and coating with chitosan31,32 had a significant positive impact on fibrosis reduction. The present study intends to propose an alternative strategy to reduce fibrosis after the transplantation of microencapsulated insulin producing cells by covalent conjugation of antiinflammatory drug on the alginate backbone allowing local controlled release from the surface of implanted microcapsules based on the hydrolytic properties of the covalent linkage in vivo. Ketoprofen is a non-steroidal anti-inflammatory drug exhibiting therapeutic effects which are mostly associated with the inhibition of cyclo-oxygenase I and II (COX-1 and COX-2) involved in the early stage inflammation cascade. In 2005, Ricci et al. investigated composite microcapsules prepared from alg/poly(L-ornithine)/alg system containing ketoprofen-loaded polyester MS.33 A high burst effect was observed, associated with fast release of the active ingredient, and anti-fibrotic effect was evidenced in vivo for cell-free multicompartment device. However, the effect was not validated in cell-containing transplants and the preparation of MS implied the separate preparation of the drug-loaded capsules followed by assembly of the multi-component systems. First, we developed straightforward


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functionalization of the encapsulation polymeric material with ketoprofen derivatives allowing the formation of MS by extrusion into a Ca2+ containing gelation bath. Then, the release of ketoprofen was quantified from empty and cell-loaded microcapsules followed by in vivo evaluation of both stability and anti-fibrotic effect with cell-free and insulin producing MIN6 cells containing capsules.

RESULTS AND DISCUSSION Preparation of ketoprofen derivatives for covalent conjugation to Na-alg. We previously established a robust conjugation protocol to modify the hydroxyl moieties in C3 position of the mannuronic residues and C2 position of the guluronic residues of the alg backbone enabling the grafting of PEG derivatives through a carbamate linkage.23 We envisaged the covalent functionalization of Na-alg with ketoprofen either by pegylation of the drug34,35 followed by modification of the alg hydroxyl groups, or by derivatization of ketoprofen with a lipoyl residue allowing post-conjugation to 1,2-dithiolane containing alg derivatives (Scheme 1). Starting from semi-protected derivatives PEG-a and PEG-b (degree of polymerization DP= 44), coupling to ketoprofen was achieved either by esterification or amide bond formation, followed by treatment under acidic conditions to remove the tert-butyl carbamate, yielding PEG-a-KET and PEG-b-KET for conjugation to Na-alg. Alternatively, ketoprofen was coupled to tetra(ethylene glycol) derivative 1, followed by Staudinger reduction of the terminal azide to provide intermediate 2 in 39% yield (2 steps). Conjugation to lipoic acid through amide bond formation afforded KET-TEG-LA in good yield.



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Scheme 1. Synthesis of ketoprofen derivatives for conjugation to Na-alg. 1. ketoprofen DCC, DMAP or HOBt, EDCI 2. HCl 4N, dioxane

O

BocHN

XH

n

PEG-a (X = O) PEG-b (X = NH) O O

H2N

n

Ph

X O

PEG-a-KET (X = O), 88% PEG-b-KET (X = NH), 76%

O

N3

NH2

3

1. EDCI, HOBt, NEt3 ketoprofen 2. PPh3 39%

1 O H2N

O

Ph

N 3 H O 2 HO2C

S S

EDCI, HOBt (iPr)2NEt 70% S S

O O

N H

O

Ph

3 N H O

KET-TEG-LA

Evaluation of anti-fibrotic effect of ketoprofen derivatives. The potential anti-fibrotic effect of ketoprofen was investigated prior to conjugation to Na-alg. Primary human fibroblasts were stimulated with the pro-fibrotic transforming growth factor beta 1 (TGFβ1) to differentiate into myofibroblasts, the effector cells of fibrosis. As shown in Figure 1, 24h after TGFβ1 treatment, human fibroblasts strongly expressed α-smooth muscle actin (α-SMA), a marker for myofibroblasts, whereas the expression level of alpha-1 type I collagen (COL1A1) 6 ACS Paragon Plus Environment

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and of matrix metalloproteinase-1 (MMP-1), two components of the extracellular matrix, remained unchanged. Incubation with KET-TEG-LA at concentrations of 0.125 mg/mL and 0.25 mg/mL did not affect the expression level of the genes. However, at a concentration of 0.5 mg/mL and 1 mg/mL the expression level of α-SMA was inhibited. Furthermore, COL1A1 expression was decreased and the expression of MMP-1, an anti-fibrotic molecule, slightly increased. This result shows that KET-TEG-LA is effective in the inhibition of αSMA and COL1A1 expression, two markers of fibrotic tissue, with optimal concentration of 0.5 mg/mL. We thus hypothesized that conjugation of ketoprofen derivatives to the encapsulation polymeric material should reduce the formation of pericapsular fibrotic tissue.

Figure 1. mRNA expression of fibrotic and anti-fibrotic molecules in human fibroblasts. Quantitative RT-PCR was performed to assess the expression of α-SMA, COL1A1 and MMP1 after 24 h stimulation with TGFβ1 (10 ng/mL) (white bars) and in the presence of KET-TEG-LA at increasing concentrations (0.125, 0.25, 0.5, 1 mg/mL) (grey bars). The dashed line indicates the expression level obtained in fibroblasts cultured in medium without TGFβ1 treatment, which was set as 1. Data from 2 independent experiments are presented as means ± SEM.



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Functionalization of Na-alg with PEG derivatives. First attempts focused on postconjugation of KET-TEG-LA to alg derivative grafted with 1,2-dithiolane-terminated PEG chains,23 aiming at the formation of disulfide clusters by mixing the two partners, with or without addition of dithiothreitol (DTT).36 As the presence of ketoprofen on the resulting hydrogels could not be evidenced, we turned our attention to the grafting of PEGylated ketoprofen derivatives on the hydroxyl groups of the alg backbone (Scheme 2). Following a recently established protocol,23 tetrabutyl ammonium (TBA)-alg was treated with 1,1'carbodiimidazole (CDI) and reacted with either PEG-a-KET or PEG-b-KET (0.1 equiv.) to produce functionalized alginate derivatives which were purified by dialysis. Under those conditions, the grafting degree of pegylated KET to the alginate hydroxyl groups was evaluated to 7% (supporting information S16, Fig. S1). Using a higher amount of PEG-a-KET and PEG-b-KET (0.2 equiv.) resulted in 20% grafting degree.

Scheme 2. Functionalization of Na-alg with pegylated ketoprofen derivatives.


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The expected chemical structures were confirmed by NMR spectroscopy. The 1H-NMR spectrum of Alg-PEG-a-KET (supporting information S13) displayed characteristic signals at 7.76-7.51 (multiplet) and 1.46 (doublet) ppm for aromatic and methyl groups of ketoprofen. A large signal between 4.10 and 3.40 pm accounts for the PEG CH2 units and the protons of the alg backbone. Similar signals were observed in the 1H-NMR spectrum of Alg-PEG-b-KET (supporting information S15). Diffusion Ordered Spectroscopy (DOSY) was performed to confirm that pegylated ketoprofen derivatives were covalently conjugated to the alginate backbone (supporting information S14).

Microsphere formation and quantification of ketoprofen release. Depending on the nature of the covalent bond to ketoprofen (ester, X = O; amide, X = NH), we expected different rates of release from the polymeric materials. First, empty microspheres were produced by extruding solutions of Alg-PEG-a-KET (7% grafting degree, 3 wt %, 1 mL) or Alg-PEG-bKET (7% grafting degree, 2.5 wt %, 1.2 mL) in 3-(N-morpholino) propanesulfonic acid (MOPS) (100 mM, pH = 7.4), into a gelation bath containing CaCl2 as ionic crosslinker. MS were kept in MOPS solution (3 mL) containing CaCl2 (100 mM) and quantification of ketoprofen release was performed over one week by LC-MS analysis of aliquots from the supernatant at regular time points (0.5, 1, 3, 6, 24, 48, 72, 96, 168 h). While MS functionalized with an ester linkage (Alg-PEG-a-KET) showed regular release of the drug over one week, MS functionalized with an amide linkage (Alg-PEG-b-KET) displayed a very slow release kinetic profile, with traces of the drug detected in the supernatant over one weeks (supporting information S17, Fig. S2). However, these MS showed irregular morphology and large size distribution, which prompted us to explore the production of MS from mixture of Alg-PEG-KET polymers (presenting 20% grafting degree) with native Na-alg. Regular morphology and narrow size distribution were achieved by extruding a mixture of solutions of



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Na-alg (1.5 wt %, 2 mL) and Alg-PEG-a-KET or Alg-PEG-b-KET (20% grafting degree, 3.5 wt %, 0.86 mL) in MOPS (100 mM, pH 7.4), into a gelation bath containing CaCl2 (100 mM). The resulting MS are designated as alg:Alg-PEG-a-KET and alg:Alg-PEG-b-KET, respectively. Using similar ratios, encapsulation of mouse insulinoma MIN6 cells was performed by mixing the initial solutions of polymers with cells (3x106 cells/mL of polymer solution) before the extrusion process. This one-step process delivered MS of average diameters between 500 and 600 µm, with homogeneous cells distribution within both types of functionalized alg hydrogels (Figure 2). For comparison, empty and MIN6 containing MS were produced from pure Na-alg.

Figure 2. MIN6 cells microencapsulated in Ca-alg MS (A), alg:Alg-PEG-a-KET MS (B) and alg:Alg-PEG-b-KET MS (C).

The release of ketoprofen from empty alg:Alg-PEG-a-KET MS was studied in MOPS solution (100 mM, 2 mL) containing CaCl2 (100 mM), adjusted to pH 3.0, 7.4 or 11. The release of ketoprofen was quantified by LC-MS from the supernatant at regular time points (0.5, 1, 3, 6, 24, 48, 72, 96, 168 and 336 h). At physiological pH, MS functionalized with ketoprofen through an ester linkage (alg:Alg-PEG-a-KET) showed regular release of the drug over two weeks, the covalent conjugation avoiding burst effect within the first hours 10 ACS Paragon Plus Environment

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following MS formation (Fig. 3). Under the same conditions, MS functionalized with an amide linkage (alg:Alg-PEG-b-KET) released only traces of the drug over two weeks (data not shown).

Figure 3. In vitro ketoprofen release from alg:Alg-PEG-a-KET and alg:Alg-PEG-b-KET MS. Empty MS (0.5 mL) were kept in MOPS solution (100 mM, 2 mL) containing CaCl2 (100 mM) at the indicated pH value, under slow mechanical agitation. Aliquots of the supernatant were withdrawn after 0.5, 1, 3, 6, 24, 48, 72, 96, 168 and 336 h, and analyzed by LC-MS. At each time point, fresh supernatant was added to compensate for the withdrawn volume.

Interestingly, after 14 days, both MS types were still releasing ketoprofen so that the drug effect can be expected to have a long time impact in vivo. In accordance with previous reports in the literature,37 basic conditions enhanced the rate of release from alg:Alg-PEG-a-KET MS while acidic conditions slowed down the kinetics. Empty MS remained stable over two weeks under all pH conditions (data not shown) showing the resistance of the electrostatic network toward a large range of pH.



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We next evaluated ketoprofen release from alg:Alg-PEG-a-KET MS containing MIN6 cells by maintaining the microcapsules in DMEM complete medium and withdrawing aliquots of the culture medium at regular time points (fresh culture medium is added at each time point to compensate for the withdrawn volume). Figure 4 presents ketoprofen release kinetic profiles from empty MS and MIN6 cells containing MS. The presence of cells induces the release of higher concentrations of ketoprofen over the first 7 days, which might be due to the presence of hydrolytic enzymes of the ester linkage in the cell content. In contrast to a co-encapsulation strategy which resulted in burst release of the drug,33 covalent functionalization of Na-alg with ketoprofen allowed longer-term release of the drug controlled by the hydrolysis rate of the chemical linkage (ester or amide) to the PEG grafting unit.

Figure 4. In vitro ketoprofen release from microencapsulated MIN6 cells in alg:Alg-PEG-aKET MS compared to empty alg:Alg-PEG-a-KET MS. Empty alg:Alg-PEG-a-KET MS and MIN6 microencapsulated in alg:Alg-PEG-a-KET MS were kept in DMEM complete medium. Aliquots of the supernatant were withdrawn after 0.5, 1, 3, 6, 24, 48, 72, 96, 168 and 336 h, and analyzed by LC-MS. At each time point, fresh culture medium was added to compensate for the withdrawn volume.


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In vivo assessment of functionalized MS. The ability of ketoprofen, covently linked to the polymers, to reduce inflammation at the implantation site and prevent pericapsular fibrotic overgrowth, was evaluated by the transplantation of empty MS (Na-alg, alg:Alg-PEG-a-KET and alg:Alg-PEG-b-KET) and MIN6 cells containing MS (Na-alg, alg:Alg-PEG-a-KET and alg:Alg-PEG-b-KET) in immune-competent mice, with a follow-up period of 30 days. Pure Ca-alg MS were implanted under the same conditions. Implantation was performed either in the peritoneal cavity or under the kidney capsule. At 30 days following transplantation, the abdominal cavity of mice contained only non-adherent free-floating MS as shown in fig. S4 (supporting information S20). Therefore, we retrieved a representative amount (500 µL) of transplanted MS for analysis. These MS were examined by light microscopy and showed variable thick layers of fibrotic tissue (figure 5A). Quantification revealed that the severity of cellular overgrowth was decreased on ketoprofen-modified empty Alg:Alg-PEG-a-KET (p

Anti-fibrotic effect of ketoprofen-grafted alginate ... - ACS Publications

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